Related Experiment Video
Updated: Apr 11, 2026

Experimental Endocarditis Model of Methicillin Resistant Staphylococcus aureus MRSA in Rat
Published on: June 4, 2012
Vaccination against Staphylococcus aureus experimental endocarditis using recombinant Lactococcus lactis expressing
Tiago Rafael Veloso1, Stefano Mancini1, Marlyse Giddey1
1Department of Fundamental Microbiology, University of Lausanne, CH-1015 Lausanne, Switzerland.
Lactococcus lactis expressing Staphylococcus aureus clumping factor A (ClfA) elicited protective immunity against experimental infective endocarditis. However, other antigens did not confer protection, indicating further research is needed to identify optimal S. aureus vaccine targets.
Area of Science:
- Microbiology
- Immunology
- Vaccinology
Background:
- Staphylococcus aureus is a significant pathogen causing severe human and animal infections, necessitating vaccine development.
- Lactococcus lactis, a non-pathogenic bacterium, serves as a potential vector for delivering antigens for vaccination.
Purpose of the Study:
- To evaluate the efficacy of non-living Lactococcus lactis heterologously expressing Staphylococcus aureus antigens (clumping factor A [ClfA] and fibronectin-binding protein A [FnbpA]) in eliciting immune responses and protecting against experimental infective endocarditis (IE) in rats.
Main Methods:
- Rats were immunized with non-living Lactococcus lactis engineered to express S. aureus ClfA, FnbpA, or both.
- Immune responses were assessed by measuring antibody production and cytokine profiles (IL-17A).
- Protection against S. aureus IE was evaluated using experimental infection models with S. aureus strains Newman and P8.
Main Results:
- Vaccination with L. lactis ClfA induced antibodies that inhibited S. aureus Newman binding to fibrinogen, promoted IL-17A production, and protected 68% of rats from IE.
- Immunization with L. lactis expressing FnbpA (alone or with ClfA) generated antibodies but did not prevent S. aureus P8 binding to fibrinogen or fibronectin, nor did it protect against IE.
- Constructs containing FnbpA did not enhance IL-17A production.
Conclusions:
- Lactococcus lactis is a viable antigen delivery system capable of inducing robust humoral and cellular immune responses.
- While L. lactis ClfA demonstrated protective potential against S. aureus IE, further investigation is required to identify the most effective antigens for a comprehensive S. aureus vaccine.
Related Concept Videos
Clinical Significance of Antibiotic Resistance
Staphylococcal Skin Infections
Endocarditis I: Introduction

